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Structure of 1368069-25-3
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2-Bromopyrazolo[1,5-a]pyrimidine serves as a pivotal heterocyclic scaffold for constructing bioactive molecules. This brominated pyrazolopyrimidine integrates readily into cross-coupling reactions, enabling efficient access to functionalized derivatives. The halogenated site facilitates palladium-catalyzed transformations, while the fused ring system imparts stability and defined electronic properties suitable for medicinal chemistry applications.
2-Bromopyrazolo[1,5-a]pyrimidine serves as a versatile building block in medicinal chemistry, enabling efficient late-stage functionalization via palladium-catalyzed cross-coupling reactions. Its bromine substituent facilitates reliable C–C and C–heteroatom bond formation under standard conditions, while the fused pyrazolo[1,5-a]pyrimidine core provides structural rigidity and favorable electronic properties for target-oriented synthesis. The compound exhibits excellent bench stability and compatibility with diverse functional groups, making it well-suited for modular scaffold development in drug discovery programs.
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GHS Pictogram :
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GHS No : GHS06
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H301-H311-H331
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P361-P405-P501
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Lot numbers can be found on the outside label of a product: